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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **1201 - 1225** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
51167	cytochrome b5 reductase 4	CYB5R4 Aliases: b5+b5R dJ676J13.1	Homo sapiens (human)	breast cancer diabetes mellitus diabetic ketoacidosis gestational diabetes glucose intolerance maturity-onset diabetes of the young prediabetes syndrome type 2 diabetes mellitus
1727	cytochrome b5 reductase 3	CYB5R3 Aliases: B5R NADH-cytochrome b5 reductase 3	Homo sapiens (human)	acquired polycythemia alternating hemiplegia of childhood autonomic neuropathy bladder urothelial carcinoma brain disease breast cancer breast carcinoma cancer central nervous system disease colon cancer colonic benign neoplasm colorectal cancer contagious pustular dermatitis cowpox dystonia embryoma epilepsy erythema infectiosum erythropoietin polycythemia esotropia essential hypertension estrogen-receptor negative breast cancer exanthema subitum familial erythrocytosis 2 familial hyperlipidemia hypertension hypertropia idiopathic scoliosis intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia locked-in syndrome maple syrup urine disease mechanical strabismus methemoglobinemia microcephaly milker's nodule monocular esotropia movement disease nervous system disease ophthalmoplegia placental insufficiency polycythemia vera polycythemia quadriplegia sickle cell anemia smallpox strabismus stress polycythemia sulfhemoglobinemia syndromic X-linked intellectual disability 94 tarsal-carpal coalition syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma variola major variola minor visual epilepsy
51700	cytochrome b5 reductase 2	CYB5R2	Homo sapiens (human)	cancer giant cell glioblastoma glioblastoma nasopharynx carcinoma prostate cancer prostate carcinoma
51706	cytochrome b5 reductase 1	CYB5R1 Aliases: humb5R2	Homo sapiens (human)	cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma large intestine cancer
5476	cathepsin A	CTSA Aliases: carboxypeptidase C carboxypeptidase Y-like kininase carboxypeptidase-L deamidase lysosomal carboxypeptidase A lysosomal protective protein urinary kininase	Homo sapiens (human)	CADASIL 1 CADASIL Fabry disease GM1 gangliosidosis type 1 GM1 gangliosidosis Laron syndrome abdominal aortic aneurysm achondroplasia acquired immunodeficiency syndrome adult-onset leukoencephalopathy with axonal spheroids and pigmented glia allergic asthma aortic aneurysm aortic valve disease 2 aortic valve stenosis aspartylglucosaminuria asthma bone giant cell tumor cancer cavernous hemangioma chorioangioma chylomicron retention disease colitis colorectal cancer colorectal carcinoma corneal dystrophy embryoma epilepsy essential hypertension fucosidosis galactosialidosis gastroenteritis genital herpes glomus tumor glycoproteinosis hemangioma herpes simplex histiocytoid hemangioma human immunodeficiency virus infectious disease hyperglycemia hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis inflammatory breast carcinoma intellectual disability intramuscular hemangioma intrinsic asthma invasive ductal carcinoma kidney failure large intestine cancer learning disability lipid storage disease lung adenocarcinoma lung cancer lymphangioma lysosomal storage disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia oophoritis osteochondrodysplasia parametritis pelvic inflammatory disease pneumonia pyosalpinx recurrent corneal erosion salpingitis sensorineural hearing loss shigellosis steatotic liver disease uremia visual epilepsy
1497	cystinosin, lysosomal cystine transporter	CTNS Aliases: CTNS-LSB PQLC4 SLC66A4	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Fanconi anemia Fanconi syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia androgen insensitivity syndrome anhidrosis autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bacterial vaginosis bone disease cartilage disease cerebral degeneration cone-rod dystrophy connective tissue disease cystinosis diabetes mellitus diabetic ketoacidosis disease of metabolism distal myopathy eunuchism exocrine pancreatic insufficiency facioscapulohumeral muscular dystrophy fundus albipunctatus glomerulonephritis hypogonadism hypohidrosis hypokalemia hypophosphatemia kidney disease kidney failure limb-girdle muscular dystrophy lysosomal storage disease male infertility muscular dystrophy nephritis nephrolithiasis nephrosis obsolete asthenopia obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete constipation oculopharyngeal muscular dystrophy osteomalacia premature menopause proteinuria pyoureter recurrent corneal erosion retinal disease retinitis pigmentosa retinitis rickets spondyloepimetaphyseal dysplasia, Sponastrime type uric acid nephrolithiasis vaginitis vulvitis vulvovaginitis
1486	chitobiase	CTBS Aliases: di-N-acetylchitobiase	Homo sapiens (human)	Clouston syndrome allergic rhinitis amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer cholera colon cancer colon carcinoma colonic benign neoplasm colorectal cancer hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer liver cancer progressive muscular atrophy prostate cancer prostate carcinoma ulcerative colitis vasomotor rhinitis
10675	chondroitin sulfate proteoglycan 5	CSPG5 Aliases: NGC neuroglycan C	Homo sapiens (human)	Beckwith-Wiedemann syndrome CLOVES syndrome Japanese encephalitis Perlman syndrome Sotos syndrome dengue disease schizophrenia viral infectious disease yellow fever
1464	chondroitin sulfate proteoglycan 4	CSPG4 Aliases: CSPG4A HMW-MAA MCSP MCSPG MEL-CSPG MSK16 NG2 melanoma-associated chondroitin sulfate proteoglycan	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Pick's disease Reye syndrome Richter's syndrome Ullrich congenital muscular dystrophy X-linked ichthyosis acute lymphoblastic leukemia adult oligodendroglioma angiomyolipoma arthritis arthropathy benign mesothelioma bone osteosarcoma brain cancer brain ischemia breast cancer breast carcinoma cancer central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia childhood oligodendroglioma childhood osteosarcoma chondrosarcoma chordoma chronic lymphocytic leukemia colitis congenital merosin-deficient muscular dystrophy 1A dementia depressive disorder dysplastic nevus syndrome dysthymic disorder embryoma endometrial cancer endometrial carcinoma epithelioid sarcoma gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma ileitis ileocolitis leukemia liver cancer lymphoblastic lymphoma major depressive disorder malignant mesothelioma melancholic depression melanoma mixed glioma mixed oligodendroglioma-astrocytoma neurotic disorder obsolete melancholia obsolete ymphosarcoma obstructive sleep apnea oligodendroglioma osteoarthritis osteosarcoma pancreatic cancer relapsing-remitting multiple sclerosis sarcoma schizophrenia skin melanoma spindle cell sarcoma uterine corpus cancer
55454	chondroitin sulfate N-acetylgalactosaminyltransferase 2	CSGALNACT2 Aliases: GALNACT-2 GALNACT2 MGC40204 PRO0082 chondroitin beta1,4 N-acetylgalactosaminyltransferase 2 glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase 2	Homo sapiens (human)	Hirschsprung's disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis multiple sclerosis
55790	chondroitin sulfate N-acetylgalactosaminyltransferase 1	CSGALNACT1 Aliases: CSGalNAcT-1 ChGn FLJ11264 chondroitin beta1,4 N-acetylgalactosaminyltransferase glucuronylgalactosylproteoglycan 4-beta-N- acetylgalactosaminyltransferase	Homo sapiens (human)	Guillain-Barre syndrome Laron syndrome Miller Fisher syndrome achondroplasia anorexia nervosa breast cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer diabetic ketoacidosis large intestine cancer melanoma multiple sclerosis obsolete type 1 diabetes mellitus 9 skin melanoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus
1431	citrate synthase	CS	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Brill-Zinsser disease Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Pick's disease Poland syndrome Q fever Reye syndrome Sengers syndrome Siberian tick typhus Zollinger-Ellison syndrome adrenal gland cancer amyotrophic lateral sclerosis anaplastic astrocytoma autism spectrum disorder autistic disorder bacillary angiomatosis bacterial sepsis bipolar disorder cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral degeneration childhood cerebral astrocytoma chronic obstructive pulmonary disease congestive heart failure coronary artery disease depressive disorder dermoid cyst of ovary diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy duodenum cancer dysthymic disorder embryoma endocarditis endomyocardial fibrosis fibrillary astrocytoma gangliocytoma ganglioneuroma gemistocytic astrocytoma giant cell glioblastoma glioblastoma heart cancer high grade glioma hyperinsulinism hyperthyroidism hypertrophic cardiomyopathy hypothyroidism juvenile pilocytic astrocytoma limb ischemia major depressive disorder malaria malignant astrocytoma melancholic depression mitochondrial DNA depletion syndrome 12b mitochondrial DNA depletion syndrome mitochondrial metabolism disease mitochondrial myopathy myocardial infarction myofibrillar myopathy neuroblastoma neurotic disorder obesity obsolete melancholia obsolete ymphosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma parapsoriasis peripheral artery disease pheochromocytoma pilocytic astrocytoma primary pulmonary hypertension progressive muscular atrophy protoplasmic astrocytoma psoriasis pustulosis of palm and sole retinal degeneration rickettsialpox small intestine cancer spondylocarpotarsal synostosis syndrome spotted fever steatotic liver disease subependymal giant cell astrocytoma thyrotoxicosis trypanosomiasis type 2 diabetes mellitus typhus
51084	crystallin lambda 1	CRYL1 Aliases: GDH L-gulonate 3-dehydrogenase MGC149525 MGC149526 crystallin, lamda 1 lambda-CRY lambda-crystallin homolog	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Laron syndrome Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia Zollinger-Ellison syndrome achondroplasia acquired thrombocytopenia acute biphenotypic leukemia acute leukemia acute myeloid leukemia autoimmune disease autoimmune lymphoproliferative syndrome beta thalassemia breast cancer breast carcinoma cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cerebral degeneration cholangiocarcinoma diabetes insipidus diarrhea embryoma giardiasis hepatocellular carcinoma hyperinsulinism hypoglycemia immune system disease intrahepatic cholangiocarcinoma liver cancer liver carcinoma mood disorder neurohypophyseal diabetes insipidus perinatal necrotizing enterocolitis placental insufficiency primary hyperoxaluria prostate cancer prostate carcinoma thalassemia
131544	crystallin beta-gamma domain containing 3	CRYBG3 Aliases: DKFZp667G2110	Homo sapiens (human)	bronchus cancer bronchus carcinoma cancer embryoma lung cancer lung carcinoma
55057	crystallin beta-gamma domain containing 2	CRYBG2 Aliases: FLJ38020 beta-gamma crystallin domain containing 2	Homo sapiens (human)
202	crystallin beta-gamma domain containing 1	CRYBG1 Aliases: suppression of tumorigenicity 4	Homo sapiens (human)	allergic asthma asthma cancer intrinsic asthma melanoma multiple myeloma patent ductus arteriosus prostate cancer prostate carcinoma skin melanoma
1407	cryptochrome circadian regulator 1	CRY1	Homo sapiens (human)	delayed sleep phase syndrome
200186	CREB regulated transcription coactivator 2	CRTC2	Homo sapiens (human)	type 2 diabetes mellitus
729920	CDP-L-ribitol pyrophosphorylase A	CRPPA Aliases: 4-diphosphocytidyl-2C-methyl-D-erythritol synthase homolog (Arabidopsis) D-ribitol-5-phosphate cytidylyltransferase IspD Nip hCG_1745121 notch1-induced protein	Homo sapiens (human)	Axenfeld-Rieger syndrome Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia anemia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bilateral optic nerve hypoplasia cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy A7 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia fundus dystrophy glaucoma hydranencephaly hydrocephalus intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly macrocytic anemia microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myositis nonpapillary renal cell carcinoma obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy papillary renal cell carcinoma persistent hyperplastic primary vitreous pneumonia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion renal carcinoma renal cell carcinoma retinal detachment rippling muscle disease 2 sarcomatoid renal cell carcinoma scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
54675	cardiolipin synthase 1	CRLS1 Aliases: CLS1 GCD10 GCD10 homolog (S. cerevisiae) dJ967N21.6	Homo sapiens (human)	Coffin-Lowry syndrome adenosarcoma bilateral breast cancer breast cancer breast ductal carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma cancer colitis combined oxidative phosphorylation deficiency 57 depressive disorder dysthymic disorder gastroenteritis hepatitis C hepatocellular carcinoma ileitis ileocolitis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder mastitis melancholic depression microglandular adenosis nephroblastoma neurotic disorder obsolete melancholia paroxysmal nocturnal hemoglobinuria schizophrenia vascular dementia
80772	ceramide-1-phosphate transfer protein	CPTP Aliases: MGC10334	Homo sapiens (human)	acute pancreatitis pancreatitis
1376	carnitine palmitoyltransferase 2	CPT2 Aliases: CPTASE	Homo sapiens (human)	Chanarin-Dorfman syndrome Meckel syndrome Pearson syndrome Reye syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis attention deficit hyperactivity disorder autosomal dominant polycystic kidney disease beta thalassemia brain disease brain edema breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency carnitine palmitoyltransferase II deficiency cataract chronic fatigue syndrome chronic kidney disease clubfoot colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of metabolism embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy essential thrombocythemia familial hyperlipidemia familial periodic paralysis fibromyalgia glycogen storage disease II glycogen storage disease V hepatitis C hepatitis hepatocellular carcinoma hydrocephalus hydronephrosis hyperglycemia hypertrophic cardiomyopathy hypoglycemia influenza isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer lipid metabolism disorder liver cancer liver cirrhosis medium chain acyl-CoA dehydrogenase deficiency microcephaly mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency muscular disease myelitis myelodysplastic syndrome myocardial infarction myoglobinuria myopathy myositis neurogenic arthropathy neuroleptic malignant syndrome obesity ovarian cancer pancytopenia placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma pseudosarcomatous fibromatosis psoriatic arthritis sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction status epilepticus steatotic liver disease systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency viral infectious disease visual epilepsy
126129	carnitine palmitoyltransferase 1C	CPT1C Aliases: CATL1 CPT1P CPTIC FLJ23809	Homo sapiens (human)	Henoch-Schoenlein purpura autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer congenital hypothyroidism embryoma giant cell glioblastoma glioblastoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 73 high grade glioma hypersensitivity vasculitis hypoglycemia hypothyroidism immune system disease lung benign neoplasm melanoma multiple myeloma myxedema neuropathy obesity papillary adenocarcinoma papillary renal cell carcinoma paraplegia peripheral nervous system disease polyneuropathy skin melanoma steatotic liver disease thyroid gland papillary carcinoma
1375	carnitine palmitoyltransferase 1B	CPT1B Aliases: CPT1-M M-CPT1 carnitine O-palmitoyltransferase 1B	Homo sapiens (human)	Balo concentric sclerosis Down syndrome Pearson syndrome acute myocardial infarction adrenoleukodystrophy bladder carcinoma cancer central nervous system disease chronic recurrent multifocal osteomyelitis colitis congestive heart failure coronary thrombosis embryoma gastroenteritis hepatitis hepatocellular carcinoma ileitis ileocolitis liver cancer morbid obesity myocardial infarction narcolepsy post-traumatic stress disorder restless legs syndrome silent myocardial infarction steatotic liver disease systemic primary carnitine deficiency disease urinary bladder cancer very long chain acyl-CoA dehydrogenase deficiency
1374	carnitine palmitoyltransferase 1A	CPT1A Aliases: CPT1-L L-CPT1	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease D-bifunctional protein deficiency Niemann-Pick disease type C1 Niemann-Pick disease Pearson syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction alcoholic hepatitis alveolar rhabdomyosarcoma amnestic disorder beta thalassemia breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency cataract 4 multiple types cerebral degeneration chronic fatigue syndrome chronic kidney disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis end stage renal disease endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma essential thrombocythemia familial hyperlipidemia familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertrophic cardiomyopathy hypoglycemia inflammatory bowel disease isolated elevated serum creatine phosphokinase levels large intestine cancer lipid metabolism disorder liver cancer liver carcinoma liver cirrhosis lymphangioleiomyomatosis major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma metabolic dysfunction-associated steatohepatitis mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency multiple sclerosis myelitis myelodysplastic syndrome myocardial infarction nasopharynx carcinoma neurotic disorder obesity obsolete melancholia osteoporosis placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis renal tubular acidosis retrograde amnesia sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction skin melanoma speech disorder steatotic liver disease stomach cancer stomach carcinoma sudden infant death syndrome systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency visual epilepsy

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